Evidence map›Paper›PMID 27721678›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2016

Inaccurate quantitation of palmitate in metabolomics and isotope tracer studies due to plastics.

Cong-Hui Yao, Gao-Yuan Liu, Kui Yang, Richard W Gross, Gary J Patti

Abstract read
In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

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0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed.

  1. Article
  2. Secretory phospholipase ACommunications biology · 2025
    Article
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  4. Review
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  18. Article
  19. The key points in the pre-analytical procedures of blood and urine samples in metabolomics studies.Metabolomics : Official journal of the Metabolomic Society · 2020
    Review
  20. Chemical Discovery in the Era of Metabolomics.Journal of the American Chemical Society · 2020
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Cong-Hui YaoDepartment of Chemistry, Washington University, St. Louis, MO, USA; Department of Medicine, Washington University, St. Louis, MO, USA.
Gao-Yuan LiuDepartment of Chemistry, Washington University, St. Louis, MO, USA; Department of Internal Medicine, Division of Bioorganic and Molecular Pharmacology, Washington University, St. Louis, MO, USA.
Kui YangDepartment of Chemistry, Washington University, St. Louis, MO, USA; Department of Internal Medicine, Division of Bioorganic and Molecular Pharmacology, Washington University, St. Louis, MO, USA.
Richard W GrossDepartment of Chemistry, Washington University, St. Louis, MO, USA; Department of Internal Medicine, Division of Bioorganic and Molecular Pharmacology, Washington University, St. Louis, MO, USA.
Gary J PattiDepartment of Chemistry, Washington University, St. Louis, MO, USA; Department of Medicine, Washington University, St. Louis, MO, USA.

Funding

REGULATION OF MYOCARDIAL PHOSPHOLIPASES AND LIPASES IN DIABETIC MYOCARDIUMR01HL118639 · NHLBI · WASHINGTON UNIVERSITY · PI GROSS, RICHARD W · 2013 to 2025
$9.1M
DEVELOPING THE UNTARGETED METABOLOMIC WORKFLOW FOR HIGH-THROUGHPUT ANALYSESR01ES022181 · NIEHS · WASHINGTON UNIVERSITY · PI PATTI, GARY J · 2012 to 2016
$1.8M
CELL-SPECIFIC ISOTOPE LABELING TO TRACK INTERCELLULAR METABOLITE EXCHANGE IN CANCERR21CA191097 · NCI · WASHINGTON UNIVERSITY · PI PATTI, GARY J · 2015 to 2017
$663k
NCI NIH HHS R21 CA191097NHLBI NIH HHS R01 HL118639NIEHS NIH HHS R01 ES022181United States NCIUnited States NIEHS
6 · The paper itself

Abstract

introductionPalmitate, the typical end product released from fatty acid synthase, is of interest to many researchers performing metabolomics. Although palmitate can be readily detected by using mass spectrometry, many metabolomic platforms involve the use of plastic consumables that introduce a competing background signal of palmitate.

objectivesThe goal of this study was to quantify palmitate contamination in metabolomics and isotope tracer studies and to examine the reliability of approaches for reducing error.

methodsWe measured the quantitative error introduced by palmitate contamination from 4 vendors of plastic consumables used in combination with several different extraction solvents.

resultsThe background palmitate signal was as much as sixfold higher than the biological palmitate signal from 4 million 3T3-L1 cells. Importantly, the palmitate contamination signal was highly variable between plastic consumables (even within the same lot) and therefore could not be accurately removed by subtracting the background as measured from a blank. In addition to affecting relative and absolute quantitation, the palmitate background signal from disposable plastics also led to the underestimation of labeled palmitate in isotope tracer experiments.

conclusionWhen measuring palmitate standard solutions, the best results were obtained when glass vials and glass pipettes were used. However, much of the palmitate background signal could be eliminated by pre-rinsing plastic vials and plastic pipette tips with methanol prior to sample introduction. For isotope tracer studies, error could also be minimized by estimating palmitate enrichment from palmitoylcarnitine, which does not have a competing contamination signal from plastic consumables.

Indexed as

Isotope labelingLipidomicsPalmitatePlastic contaminationStearate

Identifiers

PMID27721678
PMCPMC5049887

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.